FDA clears new minimally invasive Life Spine device

Life Spine received FDA 510(k) clearance for its new Prolift Lateral Expandable Spacer System.

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Prolift features minimal insertion height and controlled in-situ expansion which are key in a minimally invasive expandable lateral interbody fusion.

The device will be available in several footprint and lordotic options.

“The Prolift Lateral Expandable Spacer System is a significant addition to Life Spine’s rapidly growing expandable portfolio,” said Rich Mueller, COO of Life Spine. “The device… has anatomically convex endplates and has Life Spine’s proprietary OSSEO-LOC surface technology.”

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